Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome 773584001
SNOMED CT code
| SNOMED code | 773584001 |
|---|---|
| name | Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome (disorder) |
| synonyms | Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome |
| attributes - group2 | |
| Finding site | Skeletal muscle system structure 79984008 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Hyperplasia 76197007 |
| attributes - group1 | |
| Finding site | Entire liver 181268008 |
| Associated morphology | Enlargement 442021009 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome 773584001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome 773584001 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome 773584001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome 773584001 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Abdominal organomegaly 714254003 Large liver 80515008 Congenital hepatomegaly 407000 Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome 773584001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Congenital anomaly of musculoskeletal system 73573004 Congenital hyperplasia of muscle 66042003 Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome 773584001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome 773584001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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